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首页> 外文期刊>Cell death & disease. >Circular RNA circ_0111277 attenuates human trophoblast cell invasion and migration by regulating miR-494/HTRA1/Notch-1 signal pathway in pre-eclampsia
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Circular RNA circ_0111277 attenuates human trophoblast cell invasion and migration by regulating miR-494/HTRA1/Notch-1 signal pathway in pre-eclampsia

机译:循环RNA QUIC_0111277通过调节预先印痫前的MIR-494 / HTRA1 / NOTCH-1信号途径衰减人滋养细胞侵袭和迁移

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Mounting evidence has revealed that impaired spiral artery remodeling, placental dysfunction, and inadequate trophoblast invasion are closely correlated with the etiology and pathogenesis of pre-eclampsia (PE). Moreover, defective trophoblast invasion may trigger poor maternal-fetal circulation and placental hypoxia, leading to PE. However, the detailed molecular pathology of PE remains unclear. Although circRNAs, as a new type of stable and abundant endogenous noncoding RNA, have been proven to be essential to the pathogenesis of various diseases, their role in PE requires further verification. In this context, it is necessary to unveil the roles of circRNAs in regulating the migration and invasion of extravillous trophoblasts. In this study, using quantitative real-time PCR, we confirmed that hsa_circ_0111277 was upregulated in PE placentas relative to the level in normal pregnancy placentas. In addition, positive correlations between hsa_circ_0111277 expression and PE-related factors (proteinuria level at 24?h and placental weight) were identified by Pearson's analysis based on the clinical data of 25 PE patients. Moreover, fluorescence in situ hybridization analysis illustrated that circ_0111277 was preferentially localized within the cytoplasm. Mechanistically, circ_0111277 sponged hsa-miR-494-3p in trophoblast cells to attenuate the latter's repression by regulating HTRA1/Notch-1 expression. In conclusion, trophoblast cell migration and invasion were shown to be promoted and modulated by the hsa_circ_0111277/miR-494-3p/HTRA1/Notch-1 axis, which provides useful insight for exploring a new therapeutic approach for PE.
机译:安装证据表明,螺旋动脉重塑,胎盘功能障碍和孕产量不足侵入性障碍与预普利克斯预混物(PE)的病因和发病性密切相关。此外,有缺陷的滋养细胞侵袭可能引发较差的母胎循环和胎盘缺氧,导致PE。然而,PE的详细分子病理仍然不清楚。虽然Circrnas作为一种新型的稳定和丰富的内源性非编码RNA,但已被证明对各种疾病的发病机制至关重要,但它们在PE中的作用需要进一步验证。在这种情况下,有必要推出Circrnas在调节外向滋养细胞的迁移和侵袭方面的作用。在该研究中,使用定量实时PCR,我们证实HSA_CIRC_0111277在PE胎盘相对于正常妊娠胎盘中的水平上调。此外,基于25患者的临床资料,Pearson的分析鉴定了HSA_CIRC_0111277表达和体育与蛋白尿水平的蛋白尿水平与24℃和胎盘重量)的正相关性。此外,原位杂交分析的荧光显示,循环循环循环循环循环杂交杂交分析。机械上,Circ_0111277在滋养细胞中的海绵状HSA-miR-494-3p通过调节HTRA1 / Notch-1表达来衰减后者的抑制。总之,显示滋养细胞迁移和侵袭由HSA_CIRC_0111277 / MIR-494-3P / HTRA1 / NOTCH-1轴促进和调节,这为探索PE的新治疗方法提供了有用的见解。

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